NZ244493A

NZ244493A - Stabilised composition containing continuous non-aqueous liquid phase, dispersed organic particles and a stabiliser; bituminous compositions and preparatory methods

Info

Publication number: NZ244493A
Application number: NZ244493A
Authority: NZ
Inventors: Simon Hesp; John A Macdonald; Zhizhong Liang; Raymond Thomas Woodhams
Original assignee: Univ Toronto
Priority date: 1991-09-30
Filing date: 1992-09-25
Publication date: 1995-08-28
Also published as: EP0606307B1; WO1993007219A1; HU9400911D0; IL103272A; US5708061A; MX9205595A; DE69230339D1; US5705564A; IL103272A0; BR9206581A; MY110034A; CN1072939A; FI108144B; UA41284C2; CN1060193C; EP0606307A1; CZ75194A3; SK282319B6; CZ292016B6; CN1285377A

Abstract

Insoluble particulate materials, which may be in solid or liquid form, are dispersed in a continuous non-aqueous phase and the dispersion rendered stable and resistant to phase separation by an in-situ stabilization procedure involving the formation of chemical bonds among the stabilizer components and to dispersed phases to form a network surrounding the particles which is compatible with the continuous phase. The invention has particular application for the formation of stabilized polyolefin-modified bitumen compositions for paving and other applications.

Description

<div class="application article clearfix" id="description"> 7 L L A 0 "X A*., ; g i CJ %J Priority Dats(s): .. .V. Complete v;iC 7. Ion Filed: . 2.C. ClfCR; /59ir,sl'.*v Publication Date: . .2.5.AV.GJ.995 No.: Date: NEW ZEALAND PATENTS ACT, 1953 N.Z. PATENT O.-- "/CP 25 SEP 1992 REcavso COMPLETE SPECIFICATION IN-SITU STABILIZED COMPOSITIONS 0 We, THE UNIVERSITY OF TORONTO INNOVATIONS FOUNDATION, a no- share corporation of the Province of Ontario claiming not for profit status, of 525 University Avenue, Suite 925, Toronto, Ontario, Canada, M5G 2L3, hereby declare the invention for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:- - 1 - (followed by page - la - ) 4. i. t") la FIELD OF INVENTION 5 The present invention relates to stabilizing insoluble particulate materials in liquid phases by an in-situ reaction. REFERENCE TO RELATED APPLICATION This application is a continuation-in-part of United 10 States patent application Serial No. 767,941 filed September 30, 1991. BACKGROUND TO THE INVENTION It often is necessary to maintain insoluble solid phase particulates or immiscible liquid phase droplets in 15 suspension in a continuous liquid phase for a variety of purposes and emulsifiers of various type have been used to achieve such results. One common application is the emulsification of non-polar liquid hydrocarbons in water, in which the individual liquid hydrocarbon droplets 20 remain discrete due to electrostatic repulsion of the adsorbed emulsifiers at the droplet interface. In non-aqueous emulsions, there are no electrostatic forces and hence alternative methods must be employed to prevent coalescence and separation of the dispersed 25 phase. One specific problem area in the latter category is the provision of stabilized bitumen-polymer compositions for use as a road surface asphalt and related uses. It is well known that certain characteristics of 30 bitumens can be improved by modification by or addition of polymeric materials. For example, European Patent Publication No. 317,025 to Shell Internationale Research Maatschappij BV, discloses a bitumen composition useful in road paving applications containing an asymmetric 35 radial block copolymer which exhibits increased toughness and tenacity. Recently published PCT Publication No. WO 90/02776, to Societe Nationale Elf Aquitaine discloses 2 4 4 9 3 2 bitumens modified with a copolymer of styrene and a conjugated diene and a coupling agent, such as sulfur. Among the properties of the bitumen composition which potentially can be improved by dispersion of 5 polymeric materials therein, particularly in roadway applications, are increased rutting resistance, enhanced low temperature cracking resistance, improved traction, better adhesion/cohesion, elevated tensile strength as well as other benefits. However, a problem often 10 encountered with bitumen-polymer mixtures is an incompatibility of the bitumen and polymer components. Bitumens and most polymers, especially polyolefins such as polyethylene, are not readily miscible with each other in a molten state. A tendency exists for a dispersed 15 molten polymer to agglomerate and coalesce rapidly and not remain dispersed when stirring of the bitumen composition ceases. Once such phase separation occurs, the potential for the improved properties is lost. One approach to overcoming this problem has been the 20 use of another additive to form a stabilized bitumen gel as described in, for example, United States Patent No. 4,018,730 (issued April 19, 1977 to McDonald). This approach has the disadvantage of providing a thickened or jellied material, the higher viscosity of which has less 25 desirable working characteristics than is desirable for conventional uses of bitumens. More closely related to bituminous compositions obtainable with the present invention are those disclosed in, for example, United States Patent No. 4,314,921 30 (issued February 9, 1982 and assigned to Novophalt SA) and German Offenlegungsschrift 39 20 878 (published January *, 1990 and assigned to Novophalt SA) . These documents disclose specific methods of physical mixture to achieve homogenization of molten bitumens and 35 thermoplastic polymers, such as polyethylene. Such specialized mixing methods have heretofore been found to 3 be necessary because of the difficulty of obtaining adequate dispersion of polymer components in the bituminous phase to provide desired qualities in the working material produced. As described in United States 5 Patent No. 4,314,921, shearing forces which degrade the polymer are apparently necessary to achieve homogenization. Further, there is a tendency for the homogenized bitumens and polymers to undergo gross phase separation even after such homogenization, necessitating 10 continuous stirring and local or on-site preparation. Commercial applications of the Novophalt process as described in this patent thus include the addition of paving components, such as sand and gravel, to the homogenized mixture within a relatively short period of 15 time after the homogenization process is complete. United States Patent No. 4,154,710 of Maldonado et al. (issued May 15, 1979 to Elf Union) discloses a bitumen modified by heating bitumen in the presence of polyisobutene or a mixture of fatty acid esters (i.e. 20 esters of oleic acid, palmitic acid, stearic acid with high alcohols, such as lanosterol, cholesterol or isocholesterol) consisting of a natural extract of mutton suet, in the presence of sulphur. Apparently stable mixtures were obtained with the admixture of polymers, 25 such as isobutene-butadiene copolymer, ethylene-cylcopentadiene copolymer and polybutene-polyisobutene copolymers. In U.S. Patent No. 4,978,698, assigned to the assignee hereof and naming Raymond T. Woodhams as 30 inventor, there is described another approach to stabilizing the dispersed polymer phase. As described therein, an emulsifier system for providing a dispersed polyethylene phase comprises a polyethylene wax having a molecular weight of about 1000 to about 10,000 and 35 terminally functionalized with acidic groups, particularly carboxylic acid groups. Inorganic metal oxides may be provided in chemical association with the acidic groups of the polyethylene wax. While these compositions exhibit a degree of stability, phase separation often is observed to occur. 5 Other attempts to maintain a polymeric material dispersed in bitumen have involved the use of dispersing agents to improve compatibility between polymer and asphalt to resist coalescence and phase separation. However, none of these approaches has found success as a 10 viable commercial operation. For example, some of the polymeric modifiers used as dispersing agents tend to precipitate on pavement rolling equipment, causing severe paving problems. This prior art does not contemplate systems which 15 maintain insoluble or incompatible polymer particles or droplets stabilized in liquid asphalt medium by steric stabilization and which are resistant to phase separation at elevated temperatures for long periods of time under quiescent conditions, as in the present invention. 20 SUMMARY OF INVENTION We now have surprisingly found that we are able to achieve stable dispersions of insoluble polymers in bitumens which exhibit stability against phase separation in the liquid medium, in contrast to the prior art. Such 25 stability is achieved by employing a novel in-situ stabilization procedure, as described below, which results in a steric stabilization of the insoluble polymer particles as a dispersed phase in the bitumen. Such in-situ stabilization procedure is not limited 30 in its application to stabilization of a dispersed insoluble polymer phase in bitumen but has general application to the dispersion of insoluble organic particulates in a non-aqueous continuous phase. One example of application of the principles of the invention 35 is in the stabilization of particles of polyolefins in a 9 k \ ■ i 5 lubricating oil to provide improved lubricating properties. Other items of composition in which the system of the present invention is useful include inks, paints, 5 varnishes, caulks, sealants, coatings, roofing membranes, containment films, shingles, potting resins, lubricants and greases. Accordingly, in one aspect of the present invention, there is provided a stable composition comprising a 10 continuous non-aqueous liquid phase; a dispersed particulate phase of organic material insoluble in the liquid phase; and a steric stabilizer anchored to the particulate phase and soluble in the liquid phase to maintain dispersed particles of the particulate phase 15 spaced from each other in the liquid phase, so as to inhibit separation of the particulate phase from the liquid phase by progressive coalescence of dispersed particles. The particulate phase may be in the form of solid 20 particles or liquid droplets. The steric stabilizer component of the composition is formed by in-situ formation of chemical bonding among the steric stabilizer forming components and anchoring to the particulate organic material to form a specific steric layer having 25 a partially crosslinked structure of chemical bonds binding the liquid phase and particulate phase in spaced relation. BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a high magnification (x 1650) photograph 30 of a sample of a bitumen-polyethylene composition prepared according to the method of Example 1 described below and not in accordance with the invention, showing the presence of coalesced polyethylene particles in the bitumen as they appear after holding for 3 hours at 160°C 35 without stirring; 6 Figure 2 is a high magnification (x 1650) photograph of a sample polyethylene-bitumen composition stabilized against gross phase separation as obtained using the method of Example 3 according to the invention, after 3 5 days at 160°C without stirring; and Figure 3 is a high magnification (x 1650) photograph of a stable polyethylene-bitumen dispersion as obtained using the method of Example 3 according to the invention, after repeated reheating of the sample from room 10 temperature to 160°C, three times without stirring. GENERAL DESCRIPTION OF THE INVENTION The present invention is broadly directed to the stabilization of insoluble particulates in a non-aqueous continuous phase by the formation in-situ of chemical 15 bonding and cross-linking between the non-aqueous continuous phase and the insoluble particulates. A major application of the principles of the present invention is in the provision of stabilized polymer-modified bitumen compositions suitable for use as a 20 paving material for all paving applications, including hot mix, cut-backs, emulsions and crack fillers, as well as other uses. The term "bitumen" used herein means a class of black or dark-colored (solid, semi-solid or viscous) cementitious substances, natural or 25 manufactured, composed principally of high molecular weight hydrocarbons of which asphalts, tars, pitches and asphalites are typical. The term "asphalt" used herein means a dark, brown to black, cementitious material, solid or semi-solid in consistency, in which the 30 predominating constituents are bitumens that occur in nature, as such, or are obtained as residue in petroleum refining. The bitumen comprises the major continuous phase of the polymer-modified bitumen compositions and the polymer 35 is dispersed in the bitumen, either as solid particles or 7 liquid droplets, depending on the nature of the polymer and the temperature of the composition. The polymer component of the bitumen composition may be any polymer which can be melted or particulated for 5 dispersion in the bitumen and which imparts useful properties thereto. Generally, such polymer component comprises homopolymers and copolymers of ethylene and propylene, particularly homopolymers and copolymers of ethylene. However, other polymeric materials, such as 10 crumb rubber, may be employed. Virtually any grade of polyethylene polymer or copolymer may be used to provide the polymer component of the bitumen composition. One advantage provided by the present invention as it is applied to bitumen-polyolefin 15 and other such compositions, is the ability to employ comingled, recycled or waste polyolefins in providing the dispersed polyolefin phase, rather than requiring virgin material. For the purpose of formation of the stable emulsion 20 herein, bitumen is heated to a temperature above the fusion temperature of the polyethylene or other olefin polymer, which then is dispersed in the bitumen by high shear mixing to form a uniform dispersed phase of liquid droplets in the bitumen, which, in the presence of a 25 stabilizer, remain dispersed, when the high shear mixing ceases. However, any other convenient procedure for effecting dispersion of the particulate polymer phase may be employed. The quantity of polyethylene or other polymer dispersed in the bitumens may vary widely, 30 depending on the properties desired and the end use to which the composition is to be put. Generally, for road pavement, the quantity of polymeric material present in the composition varies from about 0.5 to about 10 wt% of the bitumen, preferably about 2.5 to about 7 wt% of the 35 bitumen. *) 8 While the bitumen is hot and the liquid droplets of polyethylene are uniformly dispersed by the shear forces applied thereto, the emulsion is stabilized in-situ by the chemical reactions described in more detail below. 5 When such reactions are complete and the shear forces are removed, the polyethylene-modified bitumen composition shows no tendency to phase separate at elevated temperatures in the range of about 100° to 200°C and remains stable in the absence of stirring. A photograph 10 of a sample of composition provided in accordance with the invention is seen in Figure 2, from which the dispersed nature of the small polyethylene droplets can be seen. This situation is to be contrasted with the photograph of Figure l, which depicts the situation only 15 a few hours after removal of stirring from a composition formed by high shear mixing but not stabilized in accordance with the present invention. An additional benefit which is achieved by the steric stabilization of the polyethylene or other olefin 20 polymer achieved herein is that small discrete particles of polyethylene are spontaneously created by dispersion of the molten polymer, with a particle size which can be adjustable to obtain different average particle sizes as required, and may be less than one micron, which is an 25 important attribute to toughness of a pavement or other end use of the composition. It is noted that simple mixing does not achieve such small dimensions, even when high shear conditions are employed, unless some dispersing agents are employed, for example, to lower 30 interfacial tension and differences in viscosity between dispersed phase and continuous phase. The composition also may be cooled to ambient temperature, may be reheated up to about 160°C or more up to about 200°C several times and may be maintained at 35 such high temperature for several days, without any tendency to phase separation. A photograph of a sample of composition which has been heated up three times to 160°C from room temperature is seen in Figure 3. As can be seen, the small polyethylene droplets remain dispersed. This attribute is important, since on-site 5 formation of the polyethylene-modified bitumen composition is not required, in contrast to the situation which exists with high-sheared non-stabilized compositions. The emulsion is inherently stable by reason of the chemical bonding and hence may be 10 solidified and reheated without loss of uniformity or stability. The composition of the invention may be formulated for use in a number of ways. As discussed below, a stabilized concentrate may be formed with which bitumen 15 and polyethylene is mixed on site. Alternatively, a composition may be provided containing the bitumen and stabilizer components which is shipped to the site of use and to which the polyethylene is added at the site. In addition, all components may be mixed at the same 20 location to form the composition. STERIC STABILIZATION For the purpose of achieving stabilization of dispersed polyethylene or other olefin polymer in bitumen, it is necessary to achieve reaction of a number 25 of components with each other and association with the continuous and dispersed phases. Stabilization is achieved using a plurality of components. One component is a bitumen-soluble component comprising a bitumen-soluble first portion, generally 30 bitumen itself, partially covalently-bonded to a polymeric second portion compatible with the bitumen-soluble first portion. The bitumen-compatible organic polymer generally is alkenic and may be a conjugated diene polymer or 35 polydiene-based copolymer. Preferably, the bitumen-compatible organic polymer is a polydiene rubber having 10 a molecular weight in the range of from about 500 to about 60,000, more particularly, a polydiene rubber having a molecular weight in the range of from about 1,000 to about 12,000. Covalent linkage of the bitumen-5 compatible polymer to the bitumen may be effected by some reactive agents, which can generate free radicals, such as peroxide or elemental sulfur, with or without an accelerator and a sulfur donor. A second component is a polymeric component miscible 10 with the dispersed polymer phase so as to be anchored thereto in the stable dispersion and which also is capable of covalent bonding, such as by nucleophilic linkage with the bitumen-compatible polymeric second portion of the first component. Nucleophilic linkage is 15 derived from the reaction of a functional group having a nucleophilic heteroatom, such as 0, N or S, with an electrophilic atom, such as a carbonyl carbon in an anhydride group. The second component preferably has a similar 20 backbone structure to the dispersed phase polymer, usually polyethylene or other polyolefin, which permits the polymer chain of the second component to blend with the molten dispersed polymer particles and to become anchored thereto. The second component may have a 25 molecular weight of about 10,000 to about 1,000,000, preferably from about 50,000 to about 500,000. Covalent linkage of the functionalized polymeric component to the bitumen-compatible organic polymer is effected, usually by reaction between a nucleophilic 30 group, such as an amino group or carboxyl group, for example, provided on the bitumen-compatible organic polymer, and an electrophilic group, such as a carbonyl group, for example, present in an anhydride group, on the polymeric component miscible with organic polymer. 35 In one particular embodiment of the invention, there may be employed as the bitumen-compatible polymer, a 11 polybutadiene or polybutadiene based copolymer partially functionalized with a nucleophilic amino group and as the polymeric component miscible with the organic polymer there may be employed a functionalized polyethylene, such 5 as carboxylated polyethylene. Other known nucleophiles include hydroxy1, carboxyl and sulfhydryl and other known electrophiles include anhydrides and other carbonyl containing groups, and epoxy and isocyanate groups. The amine-terminated 10 poly(butadiene-co-acrylonitrile) of the examples is a readily-available commercial product used for exemplification of the principles herein. Other amine functionalized polydiene polymers and butadiene copolymers containing substantially polybutadiene 15 component with e.g., styrene comonomer, are just as or more suitable and effective. Further, a polydiene polymer of higher molecular weight may be more desirable as long as it is soluble or compatible at the operating temperature. 20 Other well known covalent linkages may be employed herein to bond the bitumen-compatible polymeric component and the polymeric component. Such covalent linkage may be achieved by other means, for example, a carboxylated polydiene and a carboxylated polyethylene may be linked 25 by a difunctional aminol, diamine or diol. In addition to these components, a liquid polybutadiene soluble in or compatible with the bitumen may be provided as a third component of the stabilizer. In some cases the polybutadiene or other polydiene may be 30 omitted and the combination of the functionalized polydiene and the functionalized polymer is sufficient to effect the necessary reactions to achieve steric stabilization. It is necessary that the butadiene or other chain-extendable diene or polymer be of a molecular 35 weight such that the butadiene is soluble in or compatible with the bitumen, so as to facilitate the 12 cross-linking with the other components of the stabilizer and chain extension of the butadiene upon free-radical coupling. The molecular weight (Mw) range of this third component may be from a low molecular weight, such as 5 from about 500 to about 45,000 or higher, as long as the polybutadiene or its copolymer is soluble in or compatible with the bitumen at the mixing temperature, generally from about 150° to about 200°C. The components of the stabilizer composition, after 10 addition to the stirred elevated temperature mixture of polyethylene and bitumen, are subjected to free-radical reaction, using a free-radical initiator, such as sulfur. Usually, however, it is more practical, because of viscosity considerations to form a pro-stabilizer from 15 the stabilizer composition components which has pendant polymeric chains. Upon subsequent dispersion of the polymer in the bitumen as liquid droplets at elevated temperature, the liquid polymer droplets absorb the pendant polymeric chains and the stabilizer composition 20 thereby becomes anchored to the polymer particles, providing the gel envelope described below. The functionalized polydiene rubber and functionalized polyethylene or its copolymer react to effect covalent bonding one to the other. Upon 25 initiation of the free radical reaction between the various polydiene components as well as reactive components of the bitumen phase, such as by sulfur, the polybutadiene undergoes a series of cross-linking reactions to form a gel envelope which contributes 30 significantly to the stability of the dispersed polymer particles. In this regard, the free radical reaction causes cross-linking of the polybutadiene, cross-linking of the polybutadiene to the functionalized butadiene and linking 35 to the bitumen. The net effect of these various reactions is to form an extended polybutadiene-based 13 network with a partially cross-linked structure anchored to each of the polymer particles and swollen by the bitumen phase, to provide a gel envelope about the polymer particles, which prevents coalescence of the 5 polymer particles. The various components of the steric stabilizer are chemically-interlinked with each other and anchored to the polymer particles and the polybutadiene-based layer with a cross-linked structure which is swollen by the 10 bitumen medium ensures a substantially fixed relationship of the polymer particles one to another within the continuous bitumen phase. The polybutadiene-based layer also is bonded to bitumen. The particles are prevented from approaching each other and coalescing, if molten, by 15 the gel lattice of linked polymeric chains formed around each particle which provides a steric envelope about the individual particles. The particles, when in solid form, resist flocculation or precipitation for the same reason. The compositions of the present invention may be 20 produced in any convenient manner. In one embodiment, carboxylated polyethylene, liquid polybutadiene, (as required) amino-terminated poly(butadiene-co-acrylonitrile) and elemental sulfur may be dispersed in bitumen. For a conventional hot mix asphalt paving 25 application, a preferred ratio of carboxylated polyethylene to bitumen is from about 0.1 to about 5 per cent by weight, more preferably, from about 0.3 to about 1 per cent by weight, and a preferred ratio of amino-functionalized butadiene based copolymer is from about 30 0.1 wt% to about 3 wt%, more preferably about 0.2 to about 1 wt%. The amount of liquid butadiene may be preferably in the range of about 0.1 to about 10 wt%, more preferably from about 0.4 to about 6 wt%, of bitumen. The amount of sulfur is preferably between 35 about 0.1 per cent and about 10 per cent of the total mixture, by weight, preferably about 0.2 to about 5 wt%. 14 For other application, for example, roofing, the relative proportions of components may vary. The four ingredients are added to a heated bitumen with stirring, which may comprise high shear mixing 5 conditions at about 100° to about 2 50°C, preferably about 130° to about 200°C for a suitable period of time, which may be about 0.1 to about 3.5 hours, usually about 0.25 to about 1 hour, to form a homogeneous composition, which can be termed a concentrate. The use of vacuum or inert 10 gases may be beneficial in certain instances. This concentrate constitutes one aspect of the present invention and may be shipped to the site of formation of the final blend from concentrate, additional bitumen and polyethylene. Accordingly, in this aspect of the 15 invention, there is provided a bituminous composition for forming a stable dispersion of olefinic polymer particles in a bitumen, comprising a bitumen-compatible component, and a bitumen-compatible polymer bonded to an olefinic polymeric material and dissolved in the bitumen-20 compatible component, which functions as a pro-stabilizer. Such a concentrate may be employed in the broader application of the invention to the dispersion of an insoluble organic phase in a non-aqueous liquid phase. The polyethylene requiring dispersion in the bitumen 25 is added to the concentrate at the elevated temperature, along with additional bitumen, as required, and stirring is continued until the polyethylene is dispersed into the system to form a stable polymer-asphalt composition. Pendant olefinic polymer chains on the pro-stabilizer are 30 absorbed by the molten polyethylene and thereby blend therein, so that the stabilizer material becomes anchored to the polyethylene particles. The amount of polyethylene is present in such composition is preferably between about 0.1 and 20 percent by weight, and more 35 preferably from about 1 to about 5 percent by weight, for a conventional hot mix asphalt paving application. / L i\ - \ 1 3 15 Greater or less amounts of polyethylene or other dispersed polymer may be employed depending on the end use of the composition. The present invention thus provides a stabilized 5 molten bituminous mixture having polyethylene particles which do not coalesce at elevated temperatures. The inventors have thus found that, while a stabilizer having a polyethylene portion can stabilize molten bituminous compositions having a polyethylene additive, those 10 skilled in the art would understand that other compositions having polymer additives of the same type would be stabilized against gross phase separation by this stabilizer. In this context, a polymer segment which is miscible with molten polyethylene so as to be 15 blended therein and anchored thereto and which forms stable droplets in the presence of the stabilizer, as shown in Figure 2, thus is considered to be of the same type as polyethylene. Polyethylene and poly(ethylene-co-vinyl acetate) are considered to be polymers of the same 20 type. Similarly, it will be apparent that the principles of the present invention generally are applicable to the formation of a sterically-stabilized dispersion of an insoluble dispersed particulate phase in a non-aqueous 25 liquid continuous phase. What is required is a component which can be bound to the liquid phase, a component that can be bound to the dispersed phase and a liquid phase-soluble or -compatible, crosslinkable polymer component as a stabilizing layer anchored to the dispersed phase 30 particles and surrounding each dispersed phase particle. It has been found that an effective dispersion temperature is obtained at about 10° to 50 °C above the melting or fusion temperature of the polymer being dispersed, depending on factors, such as polymer 35 molecular weight, matrix viscosity and shear force of mixing. Thus, a grade of polyethylene having a melting 16 point of 100° to 135°C can be dispersed at a temperature of from about 100°C to 250°c. Commonly found low density, linear low iensity and high density polyethylenes thus may be dispersed and stabilized by a 5 stabilizer of the present invention. Most polyethylenes used in consumer products have fusion temperatures in the acceptable range and polyethylene blends, such as are obtained as pelletized, flaked or powdered recycled material, are suitable for dispersal in bitumens and may 10 be stabilized according to the present invention. An upper limit may be placed on the time and temperature used in dispersal of a polymer in bitumen according to the disclosed embodiments of the present invention because of the lack of stability of 15 polybutadienes above about 210°C, especially in air. However, it is possible to disperse a polymer in bitumen at a temperature higher than 210°C if an inert gas, such as nitrogen, blankets the mixing process. The quantity of steric stabilizer required to 20 achieve the required stability is quite small, generally less than about 2 wt% of bitumen, depending on several factors, such as the dispersed amount of polymer and the microstructure of the steric stabilizer formed, since different butadienes with different cis and trans-25 contents and vinyl content may form different microstructures through different cross-linked extended chains. Depending on the application to which the composition is put, the amount of stabilizer may vary up to about 10 wt%. The cost of achieving the stability is 30 economically attractive. While the use of the stabilized polyethylene-modified bitumen composition as a paving material for all types of paving has been emphasized herein, the stabilized bitumen composition also finds applications in 35 preformed paving bricks, roofing membranes, shingles, waterproofing membranes, sealants, caulks, potting resins 17 and protective finishes. Paving materials generally include aggregate, such as crushed stone pebbles, sand etc. , along with the bitumen composition. Similarly, other additives to the bitumen composition are employed, 5 depending on the end use to which the invention is put. For example, a roofing material may be obtained by the addition of suitable fillers, such as asbestos, carbonates, silicas, wood fibers, mica, sulfates, clays, pigments and/or fire retardants, such as chlorinated 10 waxes. For crack-filler applications, an oxide may advantageously be added. As mentioned above, the principles of the present invention are not limited to effecting stabilization of bitumen-polyethylene compositions, but may be employed 15 for the stabilization of dispersion of a wide variety of insoluble solid phase particulate materials in a wide variety of non-aqueous liquid phase material. In the following Examples, samples of bitumen from two different sources were employed. To the extent that 20 the properties of these materials are known, they are summarized in the following Table A: 18 TABLE A Property Lloydminister Bow River 85 - 100 290 Viscosity'1', Pa s @ 100°C 0 120 °C @ 140°C @ 160 °C Density at 15°C, g mL'1 Molecular Weight*, g mol"1 Composition1, % Asphaltenes Polar Aromatics Naphthene Aromatics Saturates + Brookfield Viscometer Ebulliometry 1 ASTM D4124-86 EXAMPLES Example 1 This Example illustrates conventional high shear mixing of polyethylene and bitumen. 5 In a one liter reactor, 100 parts of asphalt (Petro-Canada Bow River, Penetration 290 - see Table A above for properties) were heated to 150°C. Two parts of low density polyethylene (Esso Chemicals LL-6101, Mn = 12,500 g mol"1, Mw = 40,000 g mol'1, Melt Index 20) then 10 were added and dispersed in the asphalt as molten liquid droplets with a high shear mixer (Brinkman Polytron Mixer) for 30 minutes at 150°C. After mixing was stopped, the dispersion of polyethylene droplets rapidly coalesced and a viscous polyethylene layer formed on the 15 surface of the liquid asphalt, which could not be readily redispersed. This lack of stability against gross phase separation, even after high shear mixing, is typical of polyolefin dispersions in asphalt. The rapid coalescence 4 .30 l. 00 0.34 0. 15 1. 026 1200 10. 8 28 . 0 43 . 1 18 . 1 1.29 0.40 0. 16 0. 07 1.015 975 10. 3 25.5 45.6 18.5 19 of the molten polyethylene particles is seen from the photograph of Figure 1. Example 2 This Example illustrates the effect of added 5 polyethylene wax to bitumen-polyethylene emulsions. In a one liter reactor, 100 parts of asphalt (Petro-Canada Bow River, Penetration 290) were heated to 150°C. Two parts of low density polyethylene (Esso Chemicals LL-6101) and 0.5 parts of a carboxylated 10 polyethylene wax (Eastman Chemicals Epolene C-16, molecular weight = 8000 g mol1, density at 25°C = 0.908 g mol"1, acid number = 5) then were added and dispersed as molten liquid droplets with a high shear mixer as in Example 1. A fine dispersion of polyethylene droplets 15 was obtained in 15 minutes due to the presence of the C-16 wax but, after mixing was stopped, the dispersion quickly separated into readily observable phases, a viscous polyethylene surface layer being visible after the sample stood for a few hours. Although the 2 0 carboxylated polyethylene wax appears to hasten dispersal of the polyethylene within the asphalt, this material apparently does not stabilize the dispersion against gross phase separation once mixing is stopped. Example 3 25 This Example illustrates the present invention. Carboxylated polyethylene (0.5 parts Du Pont Fusabond D-101, density at 25°C = 0.920 g mol'1, Melt Flow Index = 11 to 18; anhydride content = 0.07 g mole/kg of resin, base polymer is linear low density polyethylene) 30 was dispersed in 25 parts asphalt (Petro-Canada Bow River, Penetration 290) at 150°C for 30 min. Then 1.4 parts liquid polybutadiene (Ricon 134, Colorado Chemical Specialties Inc, Microstructure 80 ± 5% trans- and cis-1,4, 20 ± 5% 1,2-vinyl, molecular weight (Mw) = 12,000, 35 Acid Number (KOH/g) = nil), 0.6 parts of a liquid amine-terminated poly(butadiene-co-acrylonitrile) (ATBN) 20 (10 per cent acrylonitrile, in liquid form, catalog No. 549, Scientific Polymer Products Inc., amine equivalent weight = 1200 g/mole), and 0.2 parts elemental sulfur were added in order and mixed under high shear for 2 5 hours at a temperature between 150° and 170°C. To this stirred mixture was added 75 parts additional asphalt (Bow River 290) and 3 parts low density polyethylene (Esso Chemicals 6101, Melt Flow Index 20) . After 5 to 20 minutes dispersal of the polyethylene as liquid droplets 10 was complete and, after stirring was terminated, no visual changes in particle size and distribution of polyethylene dispersion were apparent after 3 days storage at 160°C. The retained dispersed nature of the polyethylene droplets can be seen from the photograph of 15 Figure 2. Example 4 The method of Example 3 was repeated with 3 parts of high density polyethylene (Du Pont Sclair 2914, Melt Flow Index = 45, density at 2 5°C = 0.96 g mol"1) instead 20 of 3 parts of the low density polyethylene. The resulting asphalt emulsion was stable for 3 days at 160°C without observable changes in particle size or viscosity. Example 5 The method of Example 3 was repeated using 0.5 parts 25 carboxylated polyethylene wax (Eastman Chemical Products Epolene C-16 Wax, molecular weight less than 10,000), instead of Du Pont Fusabond D-101 carboxylated polymer. This substitution also produced a stable emulsion at 160°C. This experiment demonstrates that the 30 carboxylated polyethylene component may have a relatively low molecular weight (a wax having a molecular weight less than 10,000 g/mole) as in this Example or a high molecular weight polymer (Melt Flow Index 11-18) as in Example 3. o / f* i-\' «♦«*» „ J 21 Example 6 The method of Example 3 was repeated with Lloydminster 85-100 Penetration grade asphalt (Petro-Canada Clarkson Refinery - see Table A above for 5 properties) instead of Bow River 290 asphalt. The resulting emulsion was stable at 160°C. Examples 7 to 9 The method of Example 3 was repeated with variable ratios of reactants as shown in Table 1 below (parts by 10 weight) . The compositions ^xaroplcs 7 to 9 wore all found to be stable at 160°C for at least 3 days. These Examples demonstrate that the viscosities and particle sizes of the emulsified particles may be adjusted by appropriate control of the reagent concentrations. 15 Example 10 The method of Example 3 was repeated without the addition of 0.6 part amine terminated (poly(butadiene-co-acrylonitrile)). The resulting emulsion underwent gross phase separation as evidenced by microscopic observation. 2 0 Example 11 The method of Example 3 was repeated without the addition of sulfur. The resulting emulsion was unstable against gross phase separation as evidenced by microscopic observation. 2 5 Example 12 The method of Example 3 was repeated without the addition of the liquid polybutadiene. The resulting emulsion was unstable against gross phase separation, as evidenced by microscopic observation. 3 0 Example 13 The method of Example 3 was repeated and the sample was permitted to cool to ambient temperature, then reheated up to 160°C again several times. The stability of the polyethylene dispersion in the asphalt and the 35 viscosity of the sample were not obviously changed. The reheated dispersed nature of the polyethylene droplets can be seen from the photograph of Figure 3. The results of the foregoing Examples 1 to 13 have been tabulated for convenience of reference in the following Table I: Table I Examples of Polyethylene Emulsions in Asphalt Medium Exaaples Component, ohr 1 2 3 4 5 6 7 8 9 10 11 12 13" Asphalt (Bow river 290) 100 100 100 100 100 - 100 100 100 100 100 100 100 Asphalt (Lloyd 85/100) - - - - - 100 - - - - - - - LLDPE (LL6101) 2 2 3 - 3 3 2 1 1 3 3 3 3 HDPE (DuPont2914) - - - 3 - - - - - - - - - PE-9-ma C-16 Wax+ - 0.5 0.5 0.5 1 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 LPBD" ATBN"0 Sulfur - - 1.4 0.6 0.2 1.4 0.6 0.2 1.4 0.6 0.2 1.4 0.6 0.2 0.75 0.25 0.15 4.2 1.8 0.7 0.7 0.3 0.15 1.4 0.2 1.4 0.6 0.6 0.2 1.4 0.6 0.2 Viscosity*(cP) (160"C, 50 rpm) 114 509 520 344 175 607 216 Stability no no yes yes yes yes yes yes yes no no no yes + a carboxylated polyethylene wax ° ATBN: amino terminated poly(butadiene-co-acrylonitrile), liquid, acrylonitrile 10% 00 LPBD: Liquid polybutadiene, Mw: around 12,000 * no obvious viscosity difference in viscosity of the stable samples (Examples 3 to 9) before storage and after 3 days hot storage ™ The sample in Example 3 was cooled to ambient temperature (20° to 25°C) and reheated to 160°C again, three times. 24 It should also be understood that the photographs of Figures 1 and 2 are of molten bitumen-polymer compositions at an elevated temperature. The coalesced state shown in Figure 1 illustrates a system which 5 undergoes gross phase separation. Such a system thus displays different behavior, over time, than the type of system shown in Figure 2. The Figure 1 system when dispersed, initially gives an appearance similar to that shown in Figure 2, but with time the particles, whose 10 movement is visible under a hot-stage microscope at 160°C, coalesce into the large polymer particles shown in Figure 1 as polymer droplets encounter each other. On the other hand, the system of Figure 2, although the some movement of particles is evident, does not indicate any 15 coalescence of smaller particles into larger ones such as those of Figure 1. On a larger scale, the system of Figure 1 undergoes readily observable gross phase separation while the system of Figure 2 is stabilized against such gross phase separation. It will further be 20 appreciated that the diameters of stabilized particles evident in Figure 2 are on the order of from about 0.1 to about 1 or 3 microns. SUMMARY OF DISCLOSURE In summary of this disclosure, the present invention 25 provides novel stabilized non-aqueous liquids having a dispersed particulate phase, in particular a stabilized polymer-modified bitumen composition which resists polymer phase separation in liquid bitumen medium, both at ambient and elevated temperatures, by the use of a 30 unique steric stabilization system. Modifications are possible within the scope of this invention. </div>

Claims

25 o 'i / '1 '•*& h £ ,L): 't ■' ■ What we claim is:

1. A stable composition, comprising (a) a continuous non-aqueous liquid phase; (b) a dispersed particulate phase of organic material insoluble in said liquid phase; and (c) a steric stabilizer in the form of a gel envelope surrounding and anchored to each particle in said particulate phase and comprising a cross-linked structure compatible with said liquid phase to maintain dispersed particles of said particulate phase spaced from each other in said liquid phase, so as to inhibit separation of said particulate phase from said liquid phase by progressive coalescence of dispersed particles.

2. A composition as claimed in claim 1, in which said continuous non-aqueous liquid phase is a bitumen and said dispersed phase of organic material comprises a polymeric material insoluble in said bitumen.

3. A composition as claimed in claim 2, in which said bitumen comprises an asphalt and said polymeric material comprises a homopolymer or copolymer of ethylene.

4. A composition as claimed in claim 3, in which said steric stabilizer comprises a cross-linked polydiene compatible with said asphalt and anchored to each said particle of polymeric material.

5. A composition as claimed in any one of claim 1 to 4, wherein said envelope is comprised of a plurality of elements each comprising a first individual component anchored to said particulate phase and a second individual component different from the first individual component and bonded to the first individual component, said second component being cross-linked to each other and to the liquid phase.

6. A composition as claimed in claim 5, in which said first and second components are bonded by interaction of functional groups provided on said components. 24 A 4 9 3

7. A stable composition as claimed in claim 1 substantially as hereinbefore described with reference to the Examples.

8. - A stable composition as claimed in claim 1 substantially as hereinbefore described with reference to and as illustrated in the accompanying Figures.

9. A composition for forming a stable dispersion of olefinic polymer particles in bitumen, comprising a pro-steric stabilizer dissolved in bitumen and comprising a bitumen-compatible polymer interlinked with an olefinic polymeric material.

10. A composition as claimed in claim 9, in which said bitumen compatible polymer is an alkenic polymer.

11. A composition as claimed in claim 10, in which said alkenic polymer is a polydiene.

12. A composition as claimed in any one of claims 9 to 11, in which said olefinic polymeric material is a homopolymer and/or copolymer of ethylene.

13. A composition for forming a stable dispersion of particulate organic material in a continuous non-aqueous liquid phase, as claimed in claim 9, substantially as hereinbefore described with reference to the Examples.

14. A composition for forming a stable dispersion as claimed in claim 9, substantially as hereinbefore described with reference to the Figures.

15. A method of forming a stable composition, which comprises the steps of (a) dispersing organic material in a continuous non-aqueous liquid phase in which said organic material is insoluble to form a dispersion containing particles of said organic material in the presence of steric stabilizer forming components comprising a first individual component for anchoring to said particulate phase and a second individual component different from said first component soluble in said liquid phase; and (b) effecting chemical bonding between . said steric stabilizer forming components and bonding to '244 493 said particulate organic material to form a steric stabilizer in the form of an envelope surrounding and anchored to each particle in said particulate phase and comprising a cross-linked structure compatible with the liquid phase to maintain said particulate phase spaced apart from each other in said liquid phase.

16. A method as claimed in claim 15, in which said continuous non-liquid phase is a bitumen and said organic material comprises an olefinic polymer and said olefinic polymer is dispersed in said bitumen by contacting the same with said bitumen at an elevated temperature above the fusion temperature of the olefinic polymer.

17. A method as claimed in claim 16, in which said olefinic polymer is a homopolymer and/or copolymer of ethylene having a fusion temperature which permits dispersion of said olefinic polymer as molten droplets in bitumen at a temperature of 100° to 250°C.

18. A method as claimed in claim 17, in which said homopolymer and/or copolymer of ethylene comprises polyethylene having a fusion temperature of 100° to 135°C.

19. A method as claimed in any one of claims 17 and 18, in which said steric stabilization forming components comprise a polydiene bound to an olefinic polymer compatible with said homopolymer and/or copolymer of ethylene.

20. A method as claimed in claim 19, in which said polydiene comprises a homopolymer or copolymer of butadiene, said olefinic polymer comprises a homopolymer or copolymer of ethylene and said bonding of said components is effected by interaction between amine termination on said butadiene polymer and carboxyl termination on said ethylene polymer.

21. A method as claimed in any one of claims 16 to 20 wherein additional bitumen also is added to said homogenous bituminous composition. 244493 28

22. A method of forming a stable composition as claimed in claim 15 substantially as hereinbefore described with reference to the Examples.

23. A method of forming a stable composition as claimed in claim 15 substantially as hereinbefore described with reference to and as illustrated in the accompanying Figures.

24. A stable composition whenever prepared by a method as claimed in any one of claims 15 to 23.

25. A method of forming a bituminous composition, which comprises the steps of (a) dissolving a functionalized diene in bitumen; (b) dispersing a functionalized olefinic polymer in said bitumen; and (c) reacting said functionalized olefinic polymer and said functionalized diene so as to bind one end of said olefinic polymer to said diene.

26. A method as claimed in claim 25, in which said functionalized diene is an amine-terminated polybutadiene and s;iid functionalized olefinic polymer is a carboxylated olefinic polymer.

27. A method as claimed in claim 26, in which unfunctionalized polybutadiene also is dissolved in said bitumen and said unfunctionalized polybutadiene is subjected to partial cross-linking with said functionalized polybutadiene and itself.

28. A method as claimed in claim 27, in which said partial cross-linking is initiated by a free-radical initiator.

29. A method as claimed in claim 27, in which said free-radical initiator is sulfur, with or without sulfur accelerators.

30. A method as claimed in claim 29, in which carboxylated polyethylene as the carboxylated olefinic polymer, liquid unfunctionalized polybutadiene, amine-terminated polybutadiene and elemental sulfur are dispersed in bitumen at a temperature of 100° to 2 50°C by mixing until a homogenous composition is formed in 0.25 to 2.5 hours.

31. A method as claimed in any one of claims 2 8 to 30, in which said unfunctionalized polybutadiene has a molecular weight of from 500 to 45,000 and is soluble in or compatible with bitumen at a mixing temperature of 150° to 200°C.

32. A method of forming a bituminous composition as claimed in claim 25 substantially as hereinbefore described with reference to the Examples.

33. A method of forming a bituminous composition as claimed in claim 25 substantially as hereinbefore described with reference to and as illustrated in the Figures.

34. A bituminous composition whenever prepared by the procedure of any one of claims 25 to 33. I O\jCV CA-> 'fCC OOA Dt\j 8yX& I their auttortMd Agents A J. PARK & SON.